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FDA 510(k)

SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER

K-Number: K913886 · 1992-01-24

ApplicantSony Medical Electronics Co.
Decision Date1992-01-24
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Sony Medical Electronics Co.. It received FDA 510(k) clearance on 1992-01-24 under 510(k) number K913886. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER?

SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER is a medical device that received FDA 510(k) clearance on 1992-01-24. The listed applicant is Sony Medical Electronics Co.. The 510(k) number is K913886.

When did SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER receive FDA 510(k) clearance?

SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER received FDA 510(k) clearance on 1992-01-24, under 510(k) number K913886.

Who is the listed applicant for SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER?

The FDA 510(k) record lists Sony Medical Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER?

The FDA product code for SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER is JAA.

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Other records listing Sony Medical Electronics Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K980279SONY DXC-LS1 COLOR VIDEO CAMERAK904447SONY CINE VIDEO SYSTEM SME-3500K902535SONY WBS-700H VIDEOCASSETTE RECORDER SYSTEMK901153SONY VO-5800H VIDEOCASSETTE RECORDERK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDK884008SONY CINE VIDEO SYSTEM SME-3300

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Related Devices (Code: JAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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